Association between Haloperidol use and Risk of Rheumatoid Arthritis.
Association between Haloperidol use and Risk of Rheumatoid Arthritis.
复制标题
氟哌啶醇使用与类风湿关节炎风险之间的关联。
DOI:
10.1101/2023.09.11.23295367
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发表时间:
2023
期刊:
影响因子:
--
通讯作者:
Magagnoli,Joseph
中科院分区:
文献类型:
--
作者:
Ambati,VidyaL;Cummings,TammyH;Yerramothu,Praveen;Nguyen,Joseph;Sutton,SScott;Werner,BrianC;Magagnoli,Joseph
Dear Editors, An uncontrolled case‐series reported a benefit of haloperidol in rheumatoid arthritis (RA). 1 A study of the FDA Adverse Events Reporting System reported that among RA patients there were fewer users of antipsychotic drugs, including haloperidol, and concluded that antipsychotic drugs could reduce the risk of developing RA. 2 However, these results only suggest the converse: that RA is associated with a reduced risk of antipsychotic use; they do not indicate that antipsychotics reduce the risk of RA. The same study also examined a small employee insurance database in Japan and reported an inverse temporal relationship between RA and antipsychotic drugs, including haloperidol. Limitations of these two studies include small size, unverified and incomplete records, lack of correction for sociodemographic or clinical confounders, changing time‐trends in prescriptions, and selective loss to follow‐up. Therefore, we sought to undertake a robust pharmacoepidemiologic study of whether haloperidol, an FDA‐approved drug for the treatment of schizophrenia or Tourette disorder, affects the risk of incident RA in three large nationwide health insurance databases that comprise most of the United States population. We did so with the goal of determining whether an inexpensive drug already in clinical use could be repurposed for RA, a disease that affects tens of millions of people worldwide. We studied three health insurance databases: PearlDiver Mariner (2010–2021), IBM Marketscan Research Databases (2006–2020), and Veterans Administration (VA) Health database (2001–2021)(Supporting Information: Tables S1–S4). Inclusion criteria were at least 6 months follow‐up, at least 18 years of age, schizophrenia or Tourette disorder diagnosed on two separate occasions, and treatment with antipsychotics. RA before diagnosis of schizophrenia or Tourette disorder was exclusionary (Supporting Information: Figure S1). Disease claims were identified by ICD‐9‐CM and ICD‐10‐CM codes. Drug exposure was determined by prescriptions for generic or brand versions. Time from first prescription of antipsychotics to diagnosis of RA was the dependent variable. Sensitivity analyses were performed using diagnosis of schizophrenia or Tourette disorder as the index date and flagging treatment with antipsychotics within 60 days of
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DOI:
10.1152/jappl.1989.66.2.584
发表时间:
1989
期刊:
Journal of applied physiology (Bethesda, Md. : 1985)
影响因子:
--
作者:
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影响因子:
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期刊:
Journal of applied physiology (Bethesda, Md. : 1985)
影响因子:
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